A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2865n54



Internal ID18995041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111034401..111038564hg38UCSC Ensembl
chr12:111472205..111476368hg19UCSC Ensembl
chr12:109956588..109960751hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg384164
hg194164
hg184164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv560168, nsv560167
Samples
Known GenesCUX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2865n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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